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NBIH™ Temporary Pacing Electrode Catheter

FDA UDI

Class II (US FDA UDI)

by C. R. Bard, Inc.

Identity

Trade Name
NBIH™ Temporary Pacing Electrode Catheter FDA UDI
Generic Name
Temporary cardiac pacing catheter FDA UDI
Device Name
NBIH Temporary Pacing Electrode Catheter, Bipolar FDA UDI
Model / Reference
007152P FDA UDI
Description
NBIH Temporary Pacing Electrode Catheter, Bipolar FDA UDI

Identifiers

Catalog Number
007152P FDA UDI
Primary DI / UDI-DI
00801741011283 FDA UDI
FDA Product Code
LDF FDA UDI
GMDN Term
Temporary cardiac pacing catheter FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.3680 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Catheter Gauge — 6 French FDA UDI
Length — 100 Centimeter FDA UDI

Category: Temporary cardiac pacing catheter

NBIH™ Temporary Pacing Electrode Catheter by C. R. Bard, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Temporary cardiac pacing catheter.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
C. R. Bard, Inc.

Sources (1)

  • FDA UDI c8185c8a-8b01-4eea-b32b-14172846cc28 36 fields · synced May 31, 2026